After a successful journey gathering data from 4.3 million players and over 117 years of total game play, Sea Hero Quest is now available for scientists to continue using this fantastic app as part of their research into cognition and spatial navigation: alzheimersresearchuk.org/research/for-r…

Thank you Professor Ley Sander for the opportunity to present our research!

A third person has been declared cured of HIV after receiving a blood stem cell transplant to treat his leukaemia newscientist.com/article/236013…

Most genomics research has studied people with European ancestry. Because of this lack of diversity, scientists do not have enough data about genomic variants in other populations to calculate polygenic risk scores for these groups.

Today is Rare Disease Day and it’s a day to raise awareness for the 300 Million people in the world with over 6000 rare diseases. If you or a loved one have a rare disease write it in the comments and make it seen. #RareDisease #RareDiseaseDay #RareDiseaseDay2023

I’m very thankful for the team😇

Michelle Yeoh makes history as the first Asian woman to win the Best Actress Oscar. #Oscars95 aframe.oscars.org/news/post/mich…

The Brain Conference 2023 #BrainConf23 Join us at 11.00 GMT today for the CNS DISEASES IN LOMIC COUNTRIES Session with presentations from Gagandeep Singh, Paul F. Seke Etet, Kireshnee Naidu, Stephanie Efthymiou, PhD AFHEA🇨🇾🇬🇧 and Ley Sander Register: thebrainconference.co.uk

What a lovely way to end the week! Royal Institution The Genetics Society Thank you for sharing your thoughts and experiences Güneş Taylor The Crick

📢We're looking for patients with #ATP6V0C variants and Seizures⚡️everywhere in 🌎 Look at the maps... it's called #GeoEpilepsy !🤓Ángel Aledo-Serrano #NeuroGenetics The Neurogenetics Lab ION #RareDisease Help Us! 🌈 Still many more cities to🔎 CURE Epilepsy

Now is the time to be part of data collection programs i.e. natural history studies! If you are a parent or clinician/caregiver looking after a NARS1-affected child we would appreciate your participation in our RARE-X initiative!

It's Purple Day! Thousands of people are getting involved today to raise vital funds and raise awareness of epilepsy. If you're one of them, don't forget to share your pics and tag us Epilepsy Society 💜 #GoPurpleForEpilepsy #PurpleDay

Here’s the Chest X-Ray of a young girl suffering from a condition that is now the #1 cause of death in children and adolescents in the U.S. What’s the diagnosis?

👏👏👏👏👏👏

Happy to celebrate and thank all those who have contributed to promoting UCL Brain Sciences EDI. I am so grateful for my mentors Ley Sander Stephanie Efthymiou, PhD AFHEA🇨🇾🇬🇧, Professor Houlden, The Neurogenetics Lab ION team, and most importantly, our collaborators, Dr.Kazadi’s team in 🇨🇩 UCL Queen Square Institute of Neurology UCL QS IoN Equality, Diversity & Inclusion

Dr Stephanie Efthymiou presenting ‘Biallelic variants in ARHGAP19 cause mixed demyelinating and axonal polyneuropathy’ at #EPNS2023 in Prague 🧬🧠 Stephanie Efthymiou, PhD AFHEA🇨🇾🇬🇧 EPNS UCL Queen Square Institute of Neurology UCL Brain Sciences

Amazing!!! 🔥

My first MSc student at UCL Queen Square Institute of Neurology Angela Clara-Hwang continues to make me proud! She just secured a PhD place at Harvard Medical School after going through a long application and interview process. Go girl, congratulations 👏🏻🤓🍾

Delighted to share my first 1st author paper, now published in Neurology Genetics! neurology.org/doi/10.1212/NX… This research stems from my Master's project at UCL Neurogenetics Lab. Thank you Stephanie Efthymiou, PhD AFHEA🇨🇾🇬🇧 and Prof. Henry Houlden! The Neurogenetics Lab ION Neurology Journal